FDA Import Refusal AEK-5299679-8/12/1 — WEIFANG MINGLIANG ELECTRONICS CO

WEIFANG MINGLIANG ELECTRONICS CO — FEI 3029002343

The FDA refused shipment AEK-5299679-8/12/1 from WEIFANG MINGLIANG ELECTRONICS CO (China) on Oct 16, 2024. The refused product falls under Devices — POWERED LASER SURGICAL INSTRUMENTS. Cited charges: 288,341

Refusal Details

Date
Oct 16, 2024
Country
China
Product Category
Devices
Product Code
79GEX POWERED LASER SURGICAL INSTRUMENTS
Charges
288,341

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.